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The ligational behavior of a phenolic quinolyl hydrazone towards copper(II)- ions

BACKGROUND: The heterocyclic hydrazones constitute an important class of biologically active drug molecules. The hydrazones have also been used as herbicides, insecticides, nematocides, redenticides, and plant growth regulators as well as plasticizers and stabilizers for polymers. The importance of...

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Autores principales: Seleem, Hussein S, El-Inany, Gaber A, El-Shetary, Bashir A, Mousa, Marwa A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3033234/
https://www.ncbi.nlm.nih.gov/pubmed/21223587
http://dx.doi.org/10.1186/1752-153X-5-2
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author Seleem, Hussein S
El-Inany, Gaber A
El-Shetary, Bashir A
Mousa, Marwa A
author_facet Seleem, Hussein S
El-Inany, Gaber A
El-Shetary, Bashir A
Mousa, Marwa A
author_sort Seleem, Hussein S
collection PubMed
description BACKGROUND: The heterocyclic hydrazones constitute an important class of biologically active drug molecules. The hydrazones have also been used as herbicides, insecticides, nematocides, redenticides, and plant growth regulators as well as plasticizers and stabilizers for polymers. The importance of the phenolic quinolyl hydrazones arises from incorporating the quinoline ring with the phenolic compound; 2,4-dihydroxy benzaldehyde. Quinoline ring has therapeutic and biological activities whereas, phenols have antiseptic and disinfectants activities and are used in the preparation of dyes, bakelite and drugs. The present study is planned to check the effect of the counter anions on the type and geometry of the isolated copper(II)- complexes as well as the ligational behavior of the phenolic hydrazone; 4-[(2-(4,8-dimethylquinolin-2-yl)hydrazono)methyl] benzene-1,3-diol; (H(2)L). RESULTS: A phenolic quinolyl hydrazone (H(2)L) was allowed to react with various copper(II)- salts (Cl‾, Br‾, NO(3)‾, ClO(4)‾, AcO‾, SO(4)(2-)). The reactions afforded dimeric complexes (ClO(4)‾, AcO‾ ), a binuclear complex (NO(3)‾ ) and mononuclear complexes (the others; Cl‾, Br‾, SO(4)(2-)). The isolated copper(II)- complexes have octahedral, square pyramid and square planar geometries. Also, they reflect the strong coordinating ability of NO(3)‾, Cl‾, Br‾, AcO‾ and SO(4)(2- )anions. Depending on the type of the anion, the ligand showed three different modes of bonding viz. (NN)(0 )for the mononuclear complexes (3, 4, 6), (NO)(- )with O- bridging for the dimeric complexes (1, 5) and a mixed mode [(NN)(0 )+ (NO)(- )with O- bridging] for the binuclear nitrato- complex (2). CONCLUSION: The ligational behavior of the phenolic hydrazone (H(2)L) is highly affected by the type of the anion. The isolated copper(II)- complexes reflect the strong coordinating power of the SO(4)(2-), AcO‾, Br‾, Cl‾ and NO(3)‾ anions. Also, they reflect the structural diversity (octahedral, square pyramid and square planar) depending on the type of the counter anion.
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spelling pubmed-30332342011-02-25 The ligational behavior of a phenolic quinolyl hydrazone towards copper(II)- ions Seleem, Hussein S El-Inany, Gaber A El-Shetary, Bashir A Mousa, Marwa A Chem Cent J Research Article BACKGROUND: The heterocyclic hydrazones constitute an important class of biologically active drug molecules. The hydrazones have also been used as herbicides, insecticides, nematocides, redenticides, and plant growth regulators as well as plasticizers and stabilizers for polymers. The importance of the phenolic quinolyl hydrazones arises from incorporating the quinoline ring with the phenolic compound; 2,4-dihydroxy benzaldehyde. Quinoline ring has therapeutic and biological activities whereas, phenols have antiseptic and disinfectants activities and are used in the preparation of dyes, bakelite and drugs. The present study is planned to check the effect of the counter anions on the type and geometry of the isolated copper(II)- complexes as well as the ligational behavior of the phenolic hydrazone; 4-[(2-(4,8-dimethylquinolin-2-yl)hydrazono)methyl] benzene-1,3-diol; (H(2)L). RESULTS: A phenolic quinolyl hydrazone (H(2)L) was allowed to react with various copper(II)- salts (Cl‾, Br‾, NO(3)‾, ClO(4)‾, AcO‾, SO(4)(2-)). The reactions afforded dimeric complexes (ClO(4)‾, AcO‾ ), a binuclear complex (NO(3)‾ ) and mononuclear complexes (the others; Cl‾, Br‾, SO(4)(2-)). The isolated copper(II)- complexes have octahedral, square pyramid and square planar geometries. Also, they reflect the strong coordinating ability of NO(3)‾, Cl‾, Br‾, AcO‾ and SO(4)(2- )anions. Depending on the type of the anion, the ligand showed three different modes of bonding viz. (NN)(0 )for the mononuclear complexes (3, 4, 6), (NO)(- )with O- bridging for the dimeric complexes (1, 5) and a mixed mode [(NN)(0 )+ (NO)(- )with O- bridging] for the binuclear nitrato- complex (2). CONCLUSION: The ligational behavior of the phenolic hydrazone (H(2)L) is highly affected by the type of the anion. The isolated copper(II)- complexes reflect the strong coordinating power of the SO(4)(2-), AcO‾, Br‾, Cl‾ and NO(3)‾ anions. Also, they reflect the structural diversity (octahedral, square pyramid and square planar) depending on the type of the counter anion. BioMed Central 2011-01-11 /pmc/articles/PMC3033234/ /pubmed/21223587 http://dx.doi.org/10.1186/1752-153X-5-2 Text en Copyright ©2011 Seleem et al
spellingShingle Research Article
Seleem, Hussein S
El-Inany, Gaber A
El-Shetary, Bashir A
Mousa, Marwa A
The ligational behavior of a phenolic quinolyl hydrazone towards copper(II)- ions
title The ligational behavior of a phenolic quinolyl hydrazone towards copper(II)- ions
title_full The ligational behavior of a phenolic quinolyl hydrazone towards copper(II)- ions
title_fullStr The ligational behavior of a phenolic quinolyl hydrazone towards copper(II)- ions
title_full_unstemmed The ligational behavior of a phenolic quinolyl hydrazone towards copper(II)- ions
title_short The ligational behavior of a phenolic quinolyl hydrazone towards copper(II)- ions
title_sort ligational behavior of a phenolic quinolyl hydrazone towards copper(ii)- ions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3033234/
https://www.ncbi.nlm.nih.gov/pubmed/21223587
http://dx.doi.org/10.1186/1752-153X-5-2
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